Device recall
Z-2002-2010: Microstream CAPNOLINE H O2 ADULT 25UN Part Number: 008180
FDA device recall · Class II · Oridion Medical 1987 Ltd.
Key facts
| Recall number (Z-number) | Z-2002-2010 |
|---|---|
| Recall event | 55790 |
| Product | Microstream CAPNOLINE H O2 ADULT 25UN Part Number: 008180 |
| Product code | cck |
| Recalling firm | Oridion Medical 1987 Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 21, 2012 |
| 510(k) numbers | K010024 |
| FEI number | 3001227743 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database